101-82-6 | 2-Benzylpyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$16.00	$11.00
5g	95%	in stock	$25.00	$17.00
25g	95%	in stock	$36.00	$25.00
100g	95%	in stock	$75.00	$52.00
500g	95%	in stock	$242.00	$169.00

Description

• Catalog Number: AA04258
• Chemical Name: 2-Benzylpyridine
• CAS Number: 101-82-6
• Molecular Formula: C12H11N
• Molecular Weight: 169.2224
• MDL Number: MFCD00006352
• SMILES: c1ccc(cc1)Cc1ccccn1
• NSC Number: 4033

Computed Properties

• Complexity: 138
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.8

Upstream Synthesis Route

2-Benzylpyridine is a versatile compound widely utilized in chemical synthesis as a key intermediate in various organic reactions. Its unique structure, consisting of a benzyl group attached to a pyridine ring, enables it to participate in a range of transformation processes with excellent efficiency and selectivity.One prominent application of 2-Benzylpyridine is in the field of pharmaceutical chemistry, where it serves as a valuable building block for the synthesis of bioactive molecules and pharmaceutical agents. By selectively modifying the benzyl or pyridine moieties, chemists can introduce specific functional groups or stereochemical elements into the target molecule, thereby modulating its pharmacological properties.Furthermore, 2-Benzylpyridine is commonly employed in the synthesis of complex organic compounds, such as ligands for transition metal catalysts, polymers, and natural product derivatives. Its ability to undergo various chemical reactions, including substitution, oxidation, and reduction processes, makes it a versatile and valuable tool for creating diverse molecular structures with tailored properties.Overall, the strategic use of 2-Benzylpyridine in chemical synthesis offers researchers a powerful strategy to access novel compounds and advance our understanding of organic reactivity and molecular design.

Literature

• {(E)-4-Hy-droxy-N'-[phen-yl(pyridin-2-yl-κN)methyl-idene]benzohydrazide-κN',O}bis-(nitrato-κO,O')copper(II).

  Acta crystallographica. Section E, Structure reports online 20120201

• Ruthenium(II) complexes of 2-benzoylpyridine-derived thiosemicarbazones with cytotoxic activity against human tumor cell lines.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080401

• Interaction between tetramethylcucurbit[6]uril and some pyridine derivates.

  The journal of physical chemistry. A 20070412

• Synthesis, characterization, and preliminary oxygenation studies of benzyl- and ethyl-substituted pyridine ligands of carboxylate-rich diiron(II) complexes.

  Inorganic chemistry 20060123

• Oxidation of sulfide, phosphine, and benzyl substrates tethered to N-donor pyridine ligands in carboxylate-bridged diiron(II) complexes.

  Journal of the American Chemical Society 20040324

• Reactions of an amphoteric terminal tungsten methylidyne complex.

  Journal of the American Chemical Society 20010530

• Effect of 4-(4-chlorobenzyl)pyridine on rat hepatic microsomal cytochrome P450 and drug-metabolizing enzymes in vivo and in vitro.

  Biological & pharmaceutical bulletin 20010501

• Mode of action and quantitative structure-activity correlations of tuberculostatic drugs of the isonicotinic acid hydrazide type.

  Journal of medicinal chemistry 19760401